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THE CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/ RADIOTHERAPY V2.1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000478
510(k) Type
Special
Applicant
ACCURAY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2000
Days to Decision
65 days
Submission Type
Summary

THE CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/ RADIOTHERAPY V2.1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000478
510(k) Type
Special
Applicant
ACCURAY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2000
Days to Decision
65 days
Submission Type
Summary